Taiwan FDA registration 80ce0166fc00daa9e99775bd0bb728c5
"Optical intermediary" disposable flexible electronic ureteroscope
TW: “視介”一次性電子輸尿管軟鏡
Registration details
- Analysis ID
- 80ce0166fc00daa9e99775bd0bb728c5
- Customs Code
- DHA09200165600
Company information
- Manufacturer Country
- China
- Authorized Representative
- REVO LASER CORPORATION
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Dec 02, 2024
- Expiry Date
- Dec 02, 2029
About this record
Access comprehensive regulatory information for "Optical intermediary" disposable flexible electronic ureteroscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 80ce0166fc00daa9e99775bd0bb728c5 and manufactured by Shanghai SeeGen Photoelectric Technology Co., Ltd.. The authorized representative in Taiwan is REVO LASER CORPORATION.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
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